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A Simple and Scalable Approach To Remarkably Boost the Overall Water Splitting Activity of Stainless Steel Electrocatalysts

[Image: see text] The stainless steel mesh (SSM) has received growing consideration as an electrocatalyst for efficient hydrogen and oxygen evolution reactions. Recently, the application of SSM as an oxygen evolution reaction (OER) electrocatalyst has been more promising, while its hydrogen evolutio...

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Detalles Bibliográficos
Autores principales: Gao, Yingxia, Xiong, Tuzhi, Li, Ya, Huang, Yongchao, Li, Yuping, Balogun, M.-Sadeeq Jie Tang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6777119/
https://www.ncbi.nlm.nih.gov/pubmed/31592481
http://dx.doi.org/10.1021/acsomega.9b02315
Descripción
Sumario:[Image: see text] The stainless steel mesh (SSM) has received growing consideration as an electrocatalyst for efficient hydrogen and oxygen evolution reactions. Recently, the application of SSM as an oxygen evolution reaction (OER) electrocatalyst has been more promising, while its hydrogen evolution reaction (HER) catalytic activity is very low, which definitely affects its overall water splitting activity. Herein, a simple chemical bath deposition (CBD) method followed by phosphorization is employed to significantly boost the overall water splitting performance of SSM. The CBD method could allow the voids between the SSM fibers to be filled with Ni and P. Electrocatalytic studies show that the CBD-treated and phosphorized stainless steel (denoted SSM-Ni-P) exhibits an HER overpotential of 149 mV, while the phosphorization-free CBD-treated SSM (denoted as SSM-Ni) delivers an OER overpotential of 223 mV, both at a current density of 10 mA cm(–2). An asymmetric alkaline electrolyzer assembled based on the SSM-Ni-P cathode (HER) and SSM-Ni anode (OER) achieved an onset and 10 mA cm(–2) current densities at an overall potential of 1.62 V, granting more prospects for the application of inexpensive and highly active electrocatalysts for electrocatalytic water splitting reactions.